Duties and Responsibilities

• Undertake actions necessary for quality operation within quality control and facility
• Carry out testing procedures, ensuring that all tests are performed according to established item specifications, internal and external approved test methods and protocols.
• Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
• Ensure that safety standards and cleanliness of laboratory are maintained
• Train other analysts to perform laboratory procedures and assays following the Company training procedures
• Undertake random and scheduled quality inspections of processes, premises, personnel and products
• Communicate quality related instruction as advised by the management
• Participate in internal assessments and audits where necessary
• Troubleshoot laboratory equipment problems where applicable
• Conduct assessment on new technologies and methods to make recommendations regarding their usage
• Write or document deviation reports, testing protocols, and trend analyses in a technical reports
• Develop and revise standard quality control operating procedures for the organization
• Report, conduct investigation and propose corrective actions on out of specification (OOS) test results
• Develop, calibrate, validate, and maintain quality testing methods, laboratory equipment and devices
• Participate in technical transfer of laboratory methods and equipment where applicable
• Compile and analyze quality data as per regulatory and internal requirements
• Provide appropriate paperwork for various stages of processing monitored in compliance with specifications.
• Generate, maintain and store quality records according to internal and external standards for the industry and laboratory practice
• Identify the areas to improve productivity, quality and safety and propose for improvements to the Management

Requirements and qualifications

• Bachelor’s degree in science, or a related field is essential.
• Basic working knowledge of Microsoft Office with emphasis on Excel.
• A minimum of two years’ experience as a QC Analyst in busy manufacturing setting is desirable.
• A minimum of two years experience with HPLC/GC
• Working knowledge of Laboratory management software is an added advantage.
• Practical understanding and experience of GMP and GLP
• Hands on knowledge of modern laboratory equipment, methods and best practices.
• Strong analytical and problem-solving skills.
• Good communication is essential.
• Good time management skills.
• Active team player with integrity